Stimulation of glycogen synthesis in hepatocytes by added amino acids is related to the total intracellular content of amino acids
- 1 July 1990
- journal article
- research article
- Published by Wiley in European Journal of Biochemistry
- Vol. 191 (1) , 237-243
- https://doi.org/10.1111/j.1432-1033.1990.tb19115.x
Abstract
Katz et al. [Katz, J., Golden, S. and Wals, P. A. (1976) Proc. Natl. Acad. Sci. USA 73, 3433-3437] were the first to report that in hepatocytes isolated from fasted rats and incubated with either dihydroxyacetone, glucose or other sugars, glycogen synthesis was greatly accelerated by addition of amino acids. We have looked for possible mediators responsible for this effect and have tested the effect of alanine, proline, asparagine, glutamine or a combination of ammonia with either pyruvate or lactate in activating glycogen synthesis from dihydroxyacetone. The following observations were made. 1. Stimulation of glycogen synthesis by alanine, proline or asparagine does not require production of glutamine since the effect also occurs in periportal hepatocytes which lack glutamine synthetase. 2. Under various conditions, stimulation of glycogen synthesis by added amino acids directly correlated with increases in the intracellular content of amino acids, expressed in osmotic equivalents. 3. 3-Mercaptopicolinic acid, the inhibitor of phosphoenolpyruvate carboxykinase, further enhances stimulation of glycogen synthesis by amino acids because it increases the intracellular accumulation of aspartate and glutamate. 4. The previously reported enhancement by leucine of the stimulation of glycogen synthesis by glutamine [Chen, K. S. and Lardy, H. A. (1985) J. Biol. Chem. 260, 14683-14688] can be ascribed to inhibition of urea synthesis by leucine which results in accumulation of glutamate and of ammonia, the essential activator of glutaminase. It is concluded that activation of glycogen synthesis by added amino acids is due to an increase in intracellular osmolarity following their uptake and the accumulation of intracellular catabolites. This results in an increase in hepatic volume which stimulates glycogen synthesis [Baquet, A., Hue, L., Meijer, A. J. van Woerkom, G. M. and Plomp, P. J. A. M. (1990) J. Biol. Chem. 265, 955-959].This publication has 32 references indexed in Scilit:
- Possible role for carbamyl phosphate in the control of liver glycogen synthesisBiochemical and Biophysical Research Communications, 1985
- The nature of the decreased activity of glycogen synthase phosphatase in the liver of the adrenalectomized starved ratEuropean Journal of Biochemistry, 1984
- Hepatocyte Heterogeneity in Glutamine and Ammonia Metabolism and the Role of an Intercellular Glutamine Cycle during Ureogenesis in Perfused Rat LiverEuropean Journal of Biochemistry, 1983
- Control of Rat‐Liver Glutaminase by Ammonia and pHEuropean Journal of Biochemistry, 1983
- Potassium permeability and volume control in isolated rat hepatocytesBiochimica et Biophysica Acta (BBA) - Biomembranes, 1983
- Intracellular Compartment ation and Control of Alanine Metabolism in Rat Liver Parenchymal CellsEuropean Journal of Biochemistry, 1982
- Effect of mercaptopicolinic acid and of transaminase inhibitors on glycogen synthesis by rat hepatocytesBiochemical and Biophysical Research Communications, 1979
- Glucose activation of liver glycogen synthase. Insulin-mediated restoration of glucose effect in diabetic rate is blocked by protein synthesis inhibitorBiochimica et Biophysica Acta (BBA) - General Subjects, 1979
- Mechanism of glycogenolytic action of cycloheximide in rat liverBiochemical and Biophysical Research Communications, 1978
- HIGH-YIELD PREPARATION OF ISOLATED RAT LIVER PARENCHYMAL CELLSThe Journal of cell biology, 1969